# R82 A/S – FDA Inspection, Nov 1, 2018

Source: https://www.keypedia.com/records/fda_inspections/r82-as/f25bf9f4-63b7-4a3e-ab0e-8a1332b8bd5d
Source feed: FDA_Inspections

> FDA inspection 1070529 of R82 A/S, November 01, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1070529
- Company Name: R82 A/S
- Inspection Date: 2018-11-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 839344 - 2013-06-07](https://www.keypedia.com/records/fda_inspections/r82-as/c8f263dd-b665-4c8c-bceb-577d6e7f0a13)
- FDA Inspection 697737 - 2010-10-07

## Related Officers

- [Melanie W. Pishnery](https://www.keypedia.com/people/melanie-w-pishnery/ff4846b0-ffe1-4df0-9116-4bb238866b3a)

Company: https://www.keypedia.com/companies/r82-as/e9d511e0-668f-4cf2-ae91-f6a4de786d70

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7